Project Details
Description
VX16-809-120: A Post-approval Observational Study to Evaluate the Long-term Effectiveness and Safety of Orkambi in US Patients Who Completed Study VX12-809-105 Part A
Status | Finished |
---|---|
Effective start/end date | 4/1/18 → 12/31/19 |
Funding
- VERTEX PHARMACEUTICALS INCORPORATED
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